A kind of motor neuron and its preparation method and application
A motor neuron and motor nerve technology, applied in the field of stem cell biology, can solve the problems of low efficiency, long culture time of mature motor neurons, low purity, etc., and achieve high survival rate, large scientific research application potential, and high cell viability Effect
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Embodiment 1
[0096] This embodiment discloses a method for preparing motor neurons, comprising the following steps:
[0097] S1: Differentiation of pluripotent stem cells into neuroepithelial cells;
[0098] S2: Neuroepithelial cells differentiate into motor nerve precursor cells;
[0099] S3: Motor neuron precursor cells differentiate into post-mitotic motor neurons;
[0100] S4: Post-mitotic motor neurons differentiate to mature motor neurons, that is, mature motor neurons are obtained.
[0101] Specifically, the steps are as follows:
[0102] (1) Culture of pluripotent stem cells (D-3-D0)
[0103] The pluripotent stem cells used in the experiment have undergone strict pluripotency verification (expressing various pluripotency markers, and can form teratomas including inner, middle and outer germ layers in immunodeficient mice). Pluripotent stem cells are normally cultured in their maintenance medium, the medium used is E8 or TeSR or other similar medium. In this example, human plur...
Embodiment 2
[0129] In the method of Example 1, on the 9th day of culture, the motor nerve precursor cells were frozen with the motor nerve precursor cell cryopreservation solution. The specific steps are:
[0130] Aspirate the medium, wash once with 1x DPBS (w / o Ca2+ / Mg2+), add TrypLE digestion solution, place at 37°C, 5% CO 2 Concentration, incubate in an incubator with saturated humidity for 8-12 minutes, shake gently to make the cells completely detach from the bottom of the culture dish. Transfer the cell suspension into a 1.5mL centrifuge tube, centrifuge in a handheld centrifuge for 10-15 seconds, discard the supernatant, add 1mL motor nerve precursor cell cryopreservation solution, and gently pipette 1-2 times to disperse the cells into single cells as much as possible And count, the number of frozen cells is recommended to be 2-3×106cells / tube, and stored in liquid nitrogen.
[0131] After cryopreservation of motor nerve precursor cells, the cell recovery rate reached more than ...
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